NDC 71335-0256 – Acetaminophen and Codeine Phosphate

Acetaminophen 300 mg/1; Codeine Phosphate 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-0256

Product details

Brand name
Acetaminophen and Codeine Phosphate
Generic name
Acetaminophen and Codeine Phosphate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202800
Marketed since
April 15, 2013
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Acetaminophen and Codeine Phosphate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0256-040 TABLET in 1 BOTTLE (71335-0256-0)Aug 9, 2024
71335-0256-16 TABLET in 1 BOTTLE (71335-0256-1)Jan 31, 2019
71335-0256-220 TABLET in 1 BOTTLE (71335-0256-2)Apr 6, 2018
71335-0256-330 TABLET in 1 BOTTLE (71335-0256-3)Mar 20, 2018
71335-0256-484 TABLET in 1 BOTTLE (71335-0256-4)Aug 9, 2024
71335-0256-515 TABLET in 1 BOTTLE (71335-0256-5)Apr 23, 2018
71335-0256-6120 TABLET in 1 BOTTLE (71335-0256-6)Mar 6, 2018
71335-0256-7100 TABLET in 1 BOTTLE (71335-0256-7)Aug 9, 2024
71335-0256-860 TABLET in 1 BOTTLE (71335-0256-8)Mar 1, 2018
71335-0256-990 TABLET in 1 BOTTLE (71335-0256-9)Feb 28, 2019

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